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Merck
CN

110248

Sigma-Aldrich

1-氨基-2-丙醇

93%

别名:

(±)-1-氨基-2-丙醇, (±)-异丙醇胺

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About This Item

线性分子式:
CH3CH(OH)CH2NH2
CAS号:
分子量:
75.11
Beilstein:
605275
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

蒸汽密度

2.6 (vs air)

质量水平

蒸汽压

<1 mmHg ( 20 °C)

方案

93%

杂质

7% 2-amino-1-propanol

折射率

n20/D 1.4478 (lit.)

沸点

160 °C (lit.)

mp

−2 °C (lit.)

密度

0.973 g/mL at 25 °C (lit.)

SMILES字符串

CC(O)CN

InChI

1S/C3H9NO/c1-3(5)2-4/h3,5H,2,4H2,1H3

InChI key

HXKKHQJGJAFBHI-UHFFFAOYSA-N

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一般描述

氨基-2-丙醇可用于研究温度和水含量对氨基-2-丙醇分子结构和氢键的影响,而这已通过傅里叶变换近红外(FT-NIR)光谱而被检测

应用

氨基-2-丙醇可用作制备以下物质的反应物:
  • 采用Pd(OAc)2/I2 催化剂通过氧化羰基化反应制备的5-甲基-恶唑烷酮。
  • 通过与环氧大豆油的开环和酰胺化反应制备的生物基聚氨酯。

它还可用作溶剂和模板,用于合成含有异丙醇胺外消旋混合物的层状磷酸铝。

象形图

CorrosionExclamation mark

警示用语:

Danger

危险声明

危险分类

Acute Tox. 4 Dermal - Eye Dam. 1 - Skin Corr. 1B

储存分类代码

8A - Combustible corrosive hazardous materials

WGK

WGK 1

闪点(°F)

159.8 °F - closed cup

闪点(°C)

71 °C - closed cup

个人防护装备

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter


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Dual function of racemic isopropanolamine as solvent and as template for the synthesis of a new layered aluminophosphate:[NH3CH2CH (OH) CH3] 3{\textperiodcentered} Al3P4O16
Y Hong-Ming, et al.
Journal of Solid State Chemistry, 151(1), 145-149 (2000)
An Efficient Synthesis of 2-Oxazolidinones by Palladium-catalyzed Oxidative Carbonylation of ?-Aminoalcohols and 2-Aminophenol under Mild Conditions
Fu-Wei Li, et al.
Chin. J. Chem., 23(5), 643-645 (2005)
Synthesis of bio-based polyurethanes from epoxidized soybean oil and isopropanolamine
Miao S, et al.
Journal of Applied Polymer Science, 127(3), 1929-1936 (2013)
Krzysztof Zdzisław Haufa et al.
Applied spectroscopy, 64(3), 351-358 (2010-03-13)
The effect of temperature and water content on the molecular structure and hydrogen bonding of 2-aminoethanol (2AE), 1-amino-2-propanol (2AP), and 3-amino-1-propanol (3AP) has been examined by Fourier transform near-infrared (FT-NIR) spectroscopy. The experimental spectra were analyzed using the two-dimensional (2D)
S H Ford
Biochimica et biophysica acta, 841(3), 306-317 (1985-09-06)
Two intermediate stages in cobalamin biosynthesis, amidation of carboxylic acid groups in the corrin ring and (R)-1-amino-2-propanol attachment at propionic acid position f, have been studied using cell-free extracts from the obligate anaerobe Clostridium tetanomorphum. The preparation of an incomplete

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